Remote opportunity at
Acadia Pharmaceuticals Inc.Associate Director, SAS Programming
Acadia Pharmaceuticals Inc. is hiring an Associate Director, SAS Programming to take charge of statistical programming for a designated compound on a remote basis. In this…
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About This Role
Acadia Pharmaceuticals Inc. is hiring an Associate Director, SAS Programming to take charge of statistical programming for a designated compound on a remote basis. In this full-time position, the professional will ensure that all deliverables created internally or by functional service provider and contract research organization partners meet high standards of quality, CDISC alignment, and regulatory submission readiness. The role involves formulating programming strategies, planning resources, and maintaining hands-on involvement…
Job Description
Acadia Pharmaceuticals Inc. is hiring an Associate Director, SAS Programming to take charge of statistical programming for a designated compound on a remote basis. In this full-time position, the professional will ensure that all deliverables created internally or by functional service provider and contract research organization partners meet high standards of quality, CDISC alignment, and regulatory submission readiness. The role involves formulating programming strategies, planning resources, and maintaining hands-on involvement with intricate, high-value tasks.
The person in this role will guide lead programmers, oversee vendors, and collaborate closely with cross-functional research and development teams. Ideal candidates bring extensive clinical data programming expertise within biotech or pharmaceutical settings. Acadia offers a comprehensive compensation package that includes discretionary bonuses, equity awards, and various employee benefits.
Responsibilities
- Serve as the primary programming lead for an assigned compound, overseeing timelines, quality, and deliverables across related studies
- Establish compound programming strategies covering standards, dataset design, and validation methodologies
- Develop and maintain resource plans and timelines while forecasting demand and identifying staffing gaps
- Contribute programming input for statistical analysis plans, case report forms, and data transfer specifications
- Write and validate SDTM, ADaM, and TLF programs for critical milestones including database locks, topline results, and regulatory submissions
- Design and program integrated datasets across studies to support pooled analyses and summaries of efficacy and safety
- Direct the validation strategy, oversee conformance reports, and manage rapid ad hoc analyses for leadership
- Ensure all outputs comply with regulatory requirements such as GCP, ICH, and 21 CFR Part 11, serving as compound subject matter expert during audits
- Qualify and manage CRO and FSP partners while directing external programming resources
- Partner with internal teams to drive standards, share regulatory insights, and provide technical guidance to contractors
Requirements
- Around 8 years of progressively responsible experience in clinical data statistical programming within pharmaceutical or biotechnology environments
- Experience operating as a lead programmer on multiple studies or programs alongside oversight of CRO or FSP deliverables
- Expert-level competency in SAS programming including Base SAS, SAS/STAT, SAS Macro, ODS, SAS/GRAPH, and SQL
- Comprehensive knowledge of CDISC standards such as SDTM, ADaM, controlled terminology, define.xml, and reviewer guides
- Familiarity with clinical trial data, the drug development lifecycle, and regulatory standards including GCP, ICH, 21 CFR Part 11, FDA, EMA, and PMDA requirements
- Experience constructing integrated datasets across multiple trials for safety and efficacy summaries
- Ability to utilize conformance tooling such as Pinnacle 21 and resolve findings
- Willingness and capability to travel domestically and internationally as required
Qualifications
- Bachelor degree in statistics, biostatistics, computer science, mathematics, or a related field
- Master degree in a related discipline
- SAS certification at the Advanced Programmer level
- Experience supporting NDA, BLA, or MAA submissions including data packages and health authority responses
- Working knowledge of the R programming language
- Practical application of generative AI tools to enhance programming efficiency and quality in a regulated environment
Core Skills
Benefits
- Competitive base salary ranging from USD 162,600 to 203,300 per year
- Discretionary bonus and equity awards based on individual and organizational performance
- Medical, dental, and vision insurance coverage
- Employer-paid life, disability, business travel, and employee assistance program coverage
- 401(k) plan featuring a fully vested company match up to 5 percent
- Employee Stock Purchase Plan offering a 2-year purchase price lock-in
- Fifteen or more vacation days
- Thirteen to fifteen paid holidays including a year-end office closure from December 24th through January 1st
- Ten days of paid sick leave
- Paid parental leave
- Tuition assistance
Frequently Asked Questions
Answers are based only on the employer’s listing; where it doesn’t say, neither do we.
What is the remote work policy for this position?
The source posting lists the remote status of this job as remote.
What is the salary range for the Associate Director, SAS Programming role?
The annual base salary ranges from USD 162,600 to 203,300, and the position is also eligible for discretionary bonuses and equity awards.
What level of education is required to apply?
Applicants are required to have a bachelor degree in statistics, biostatistics, computer science, mathematics, or a related field, though a master degree is preferred.
How many years of experience are targeted for this role?
The posting targets approximately 8 years of progressively responsible experience in statistical programming with clinical data within a pharmaceutical or biotech environment.
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